Liquibandfix8® Open Hernia Mesh Fixation Device
LiquiBandFIX8® Open Hernia Mesh Fixation Device Recall The LiquiBandFIX8® Open Hernia Mesh Fixation Device is being recalled across Canada because it can fail prematurely during or after hernia repair surgery. This Class I recall affects all patients who received this device for hernia repair procedures. The device is used to secure mesh implants in open hernia surgery.
- Product
- LiquiBandFIX8® Open Hernia Mesh Fixation Device
- Reason
- Premature failure
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-02-11
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/803d121d-82fc-40e5-b29f-b359d5109523